CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 260 enrolled
Drug / intervention
Not specified
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02671422
NCT02671422N/ACompleted

A Non-interventional Biomarker Study in Patients With Non-Small Cell Lung Cancer (NSCLC) of Adenocarcinoma Tumour Histology Eligible for Treatment With Vargatef® According to the Approved Label.

Boehringer Ingelheim·observational·Posted Feb 2, 2016·Updated Sep 24, 2020

In Brief

An observational study for Carcinoma, Non-Small-Cell Lung. Completed, enrolled 260 participants across 71 sites in 13 countries.

Detailed Summary

At present there are no approved predictive tumour- or serum-derived biomarkers guiding usage of anti-angiogenic therapies in patients with adenocarcinoma of NSCLC.The objective of this NIS is to examine whether genetic/genomic markers (alone or combined with clinical covariates) could be used to predict OS in NSCLC patients eligible for treatment with Vargatef®. The investigations in this study are exploratory in nature and considered to be hypothesis generating. The results from these investigations may help to expand our understanding of the disease and the response to Vargatef®.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesAustria, Belgium, Denmark, Germany, Greece, Hungary, Italy, Lithuania, Luxembourg, Netherlands, Spain, Sweden, United Kingdom
Collaborators--

Timeline

N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedFeb 2, 2016
Enrollment StartMar 9, 2016
Primary CompletionSep 3, 2019
TodayJul 2, 2026
Enrollment to primary: 3.5 yearsPosted 10.4 years ago